RGD:11662307 Rat Genome Database

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Variant: RGD:11662307 -  Homo sapiens

RGD ID: 11662307
RS ID: rs886058970
ClinVar ID: CV291881
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TACR3  TACR3-AS1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 104,510,637
GRCh38 4 103,589,480
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_023344.1:g.135337G>C
NC_000004.12:g.103589480C>G
NC_000004.11:g.104510637C>G
NM_001059.3:c.*202G>C
More... 		06/14/2016 3 prime utr variant uncertain significance HYPOGONADOTROPIC HYPOGONADISM 11 WITHOUT ANOSMIA
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TACR3
Accession:NM_001059
Location:3UTRS;EXON

Gene Symbol:TACR3-AS1
Accession:NR_186501
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000384433 CLINVAR
dbSNP (RS) rs886058970 CLINVAR
MedGen C3553844 CLINVAR
NCBI Gene TACR3 CLINVAR
  TACR3-AS1 CLINVAR
OMIM 162332 CLINVAR
  614840 CLINVAR